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rs863223977

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223977(A;T)
Make rs863223977(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241500488
GeneFH
is asnp
is mentioned by
dbSNPrs863223977
ebirs863223977
HLIrs863223977
Exacrs863223977
Varsomers863223977
Maprs863223977
PheGenIrs863223977
hapmaprs863223977
1000 genomesrs863223977
hgdprs863223977
ensemblrs863223977
gopubmedrs863223977
geneviewrs863223977
scholarrs863223977
googlers863223977
pharmgkbrs863223977
gwascentralrs863223977
openSNPrs863223977
23andMers863223977
23andMe allrs863223977
SNP Nexus

SNPshotrs863223977
SNPdbers863223977
MSV3drs863223977
GWAS Ctlgrs863223977
Max Magnitude0
ClinVar
Risk rs863223977(T;T)
Alt rs863223977(T;T)
Reference rs863223977(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241663788T>A
CLNSRC
CLNACC RCV000200236.1,